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chris克里斯

铁虫 (小有名气)

应助: 0 (幼儿园)
金币: 173.5
红花: 2
帖子: 85
在线: 10.1小时
虫号: 3472699
注册: 2014-10-13
专业: 临床药理

[交流] Global CRO公司招聘生物统计师Biostatistician - 上海

具体工作地点:

上海

薪金:

年薪20-50W

招聘岗位:

Biostatistician

联系方式:

jerryyoung6@163.com

Accountabilities
Develops statistical analysis plans and reporting specifications for simple to moderate clinical studies.
• Develops and describes appropriate statistical techniques for the analysis of data in a statistical analysis plan.
• Works with other statisticians on statistical methodology, study design, therapeutic area details, and data analysis.
• Design appropriate shells and specifications for outputs.
Performs statistical analyses and interprets results from simple to moderate clinical studies.
• Develops or QCs analysis programs to implement techniques described in the statistical analysis plan.
• Approves final database for freeze/lock.
• Assesses model assumptions for statistical analyses.
• Works with programmers, writers, and clinicians to coordinate data summarization and analysis activities, including summary statistics, tabulations, graphics, analysis output, and raw data listings.
• Develops and reviews statistical reports and statistical sections of clinical study reports.
Contributes statistical expertise to project teams for the design, analysis, and reporting of simple to moderate clinical studies.
• Serves as primary functional representative on project teams.
• Provides input into the preparation and review of clinical study protocols.
• Creates dummy and final randomization schemes for clinical studies.
• Participates in the development and review of CRFs, data edit specifications, and critical variable lists.
• Works with the project manager and functional manager to determine resource projections and project schedules.
• Visits clients to discuss statistical issues.
Maintains, develops, and shares knowledge of company and industry procedures and methodologies.
• Performs billable work in accordance with WuXiPRA’s policies, procedures, and SOPs.
• Maintains solid knowledge of drug development process.
• Maintains solid knowledge of SAS procedures and good programming practices.
• Continues statistical training on new methods and techniques via self-study, internal training and courses, and external conferences and courses.
• Trains and mentors new or junior statisticians on statistical methods and WuXiPRA procedures.
• Develops knowledge of FDA and EMEA guidelines and requirements for reporting of clinical trials data.

Qualifications
 MS degree with 3 years of experience within the clinical trials or pharmaceutical industry or PhD degree in statistics or biostatistics
 Demonstrated expertise in multiple and complex statistical areas
 Demonstrated ability to plan, implement, and monitor the statistical processes for clinical studies
 Excellent written and oral communication skills; Read, write and speak English.

If interested in this position, please send your English CV to jerryyoung6@163.com

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